Active Ingredient: IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG;30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A213565
Product Number: 001
Approval Date: Mar 10, 2023
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information